Gk2 Variant Search Result - Rat Genome Database

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49 records found for search term Gk2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155917132	CV2236474	single nucleotide variant	NM_033214.3(GK2):c.205G>A (p.Ala69Thr)	not specified [RCV004110478]	uncertain significance	4	79407996	79407996	Human		name
155929936	CV2354025	single nucleotide variant	NM_033214.3(GK2):c.272G>A (p.Ser91Asn)	not specified [RCV004204456]	uncertain significance	4	79407929	79407929	Human		name
401741156	CV2680342	single nucleotide variant	NM_033214.3(GK2):c.100G>A (p.Glu34Lys)	not specified [RCV004288594]	uncertain significance	4	79408101	79408101	Human		name
405752309	CV3251578	single nucleotide variant	NM_033214.3(GK2):c.227A>G (p.Asp76Gly)	not specified [RCV004392925]	uncertain significance	4	79407974	79407974	Human		name
405752318	CV3251579	single nucleotide variant	NM_033214.3(GK2):c.248C>T (p.Ser83Phe)	not specified [RCV004392926]	uncertain significance	4	79407953	79407953	Human		name
156058993	CV2262942	single nucleotide variant	NM_033214.3(GK2):c.447C>G (p.Phe149Leu)	not specified [RCV004125080]	uncertain significance	4	79407754	79407754	Human		name
156079691	CV2292619	single nucleotide variant	NM_033214.3(GK2):c.989G>A (p.Arg330His)	not specified [RCV004154309]	uncertain significance	4	79407212	79407212	Human		name
156395692	CV2325868	single nucleotide variant	NM_033214.3(GK2):c.377T>C (p.Leu126Pro)	not specified [RCV004174052]	uncertain significance	4	79407824	79407824	Human		name
156096918	CV2375498	single nucleotide variant	NM_033214.3(GK2):c.416C>T (p.Ser139Phe)	not specified [RCV004226009]	uncertain significance	4	79407785	79407785	Human		name
401722521	CV2677015	single nucleotide variant	NM_033214.3(GK2):c.799C>A (p.Gln267Lys)	not specified [RCV004293616]	uncertain significance	4	79407402	79407402	Human		name
401741160	CV2680343	single nucleotide variant	NM_033214.3(GK2):c.533T>C (p.Ile178Thr)	not specified [RCV004288595]	uncertain significance	4	79407668	79407668	Human		name
401772121	CV2719539	single nucleotide variant	NM_033214.3(GK2):c.751G>A (p.Val251Met)	not specified [RCV004327223]	uncertain significance	4	79407450	79407450	Human		name
405752325	CV3251580	single nucleotide variant	NM_033214.3(GK2):c.463C>G (p.Arg155Gly)	not specified [RCV004392927]	uncertain significance	4	79407738	79407738	Human		name
405752332	CV3251581	single nucleotide variant	NM_033214.3(GK2):c.490G>C (p.Val164Leu)	not specified [RCV004392928]	uncertain significance	4	79407711	79407711	Human		name
405752337	CV3251582	single nucleotide variant	NM_033214.3(GK2):c.921A>T (p.Lys307Asn)	not specified [RCV004392929]	uncertain significance	4	79407280	79407280	Human		name
407513338	CV3443290	single nucleotide variant	NM_033214.3(GK2):c.391C>A (p.Pro131Thr)	not specified [RCV004627152]	uncertain significance	4	79407810	79407810	Human		name
407513347	CV3443292	single nucleotide variant	NM_033214.3(GK2):c.472C>G (p.Leu158Val)	not specified [RCV004627154]	uncertain significance	4	79407729	79407729	Human		name
407513350	CV3443293	single nucleotide variant	NM_033214.3(GK2):c.472C>T (p.Leu158Phe)	not specified [RCV004627155]	uncertain significance	4	79407729	79407729	Human		name
407519551	CV3443294	single nucleotide variant	NM_033214.3(GK2):c.425G>A (p.Gly142Asp)	not specified [RCV004629634]	uncertain significance	4	79407776	79407776	Human		name
597707379	CV3681155	single nucleotide variant	NM_033214.3(GK2):c.303C>G (p.Asp101Glu)	not specified [RCV004917088]	uncertain significance	4	79407898	79407898	Human		name
597759592	CV3681156	single nucleotide variant	NM_033214.3(GK2):c.589A>G (p.Thr197Ala)	not specified [RCV004925537]	uncertain significance	4	79407612	79407612	Human		name
597707400	CV3681158	single nucleotide variant	NM_033214.3(GK2):c.728T>A (p.Ile243Asn)	not specified [RCV004917090]	uncertain significance	4	79407473	79407473	Human		name
598251948	CV3977751	single nucleotide variant	NM_033214.3(GK2):c.749G>A (p.Gly250Asp)	not specified [RCV005346002]	uncertain significance	4	79407452	79407452	Human		name
598251959	CV3977753	single nucleotide variant	NM_033214.3(GK2):c.448A>G (p.Ser150Gly)	not specified [RCV005346004]	uncertain significance	4	79407753	79407753	Human		name
598251965	CV3977754	single nucleotide variant	NM_033214.3(GK2):c.502G>A (p.Val168Ile)	not specified [RCV005346005]	uncertain significance	4	79407699	79407699	Human		name
598251970	CV3977755	single nucleotide variant	NM_033214.3(GK2):c.326A>T (p.Tyr109Phe)	not specified [RCV005346006]	uncertain significance	4	79407875	79407875	Human		name
598251975	CV3977756	single nucleotide variant	NM_033214.3(GK2):c.413A>T (p.Lys138Met)	not specified [RCV005346007]	uncertain significance	4	79407788	79407788	Human		name
8625852	CV80976	single nucleotide variant	NM_033214.2(GK2):c.818G>A (p.Gly273Glu)	Malignant melanoma [RCV000061054]	not provided	4	79407383	79407383	Human		name
156270377	CV2195160	single nucleotide variant	NM_033214.3(GK2):c.1469A>G (p.Gln490Arg)	not specified [RCV004080108]	uncertain significance	4	79406732	79406732	Human		name
156381586	CV2215637	single nucleotide variant	NM_033214.3(GK2):c.1171C>T (p.His391Tyr)	not specified [RCV004089388]	uncertain significance	4	79407030	79407030	Human		name
156170968	CV2312546	single nucleotide variant	NM_033214.3(GK2):c.1452G>A (p.Met484Ile)	not specified [RCV004169291]	uncertain significance	4	79406749	79406749	Human		name
156164232	CV2315071	single nucleotide variant	NM_033214.3(GK2):c.1504A>G (p.Thr502Ala)	not specified [RCV004165263]	uncertain significance	4	79406697	79406697	Human		name
156325185	CV2335181	single nucleotide variant	NM_033214.3(GK2):c.1167A>T (p.Lys389Asn)	not specified [RCV004184709]	uncertain significance	4	79407034	79407034	Human		name
156045611	CV2397265	single nucleotide variant	NM_033214.3(GK2):c.1606A>T (p.Ile536Leu)	not specified [RCV004238799]	uncertain significance	4	79406595	79406595	Human		name
405752297	CV3251576	single nucleotide variant	NM_033214.3(GK2):c.1505C>T (p.Thr502Ile)	not specified [RCV004392923]	uncertain significance	4	79406696	79406696	Human		name
405752304	CV3251577	single nucleotide variant	NM_033214.3(GK2):c.1524G>A (p.Met508Ile)	not specified [RCV004392924]	uncertain significance	4	79406677	79406677	Human		name
407513345	CV3443291	single nucleotide variant	NM_033214.3(GK2):c.1496G>A (p.Arg499His)	not specified [RCV004627153]	uncertain significance	4	79406705	79406705	Human		name
597759583	CV3681151	single nucleotide variant	NM_033214.3(GK2):c.1020G>C (p.Glu340Asp)	not specified [RCV004925535]	uncertain significance	4	79407181	79407181	Human		name
597759587	CV3681152	single nucleotide variant	NM_033214.3(GK2):c.1322T>C (p.Ile441Thr)	not specified [RCV004925536]	uncertain significance	4	79406879	79406879	Human		name
597707362	CV3681153	single nucleotide variant	NM_033214.3(GK2):c.1423G>C (p.Glu475Gln)	not specified [RCV004917086]	uncertain significance	4	79406778	79406778	Human		name
597707370	CV3681154	single nucleotide variant	NM_033214.3(GK2):c.1103A>G (p.Tyr368Cys)	not specified [RCV004917087]	uncertain significance	4	79407098	79407098	Human		name
597707391	CV3681157	single nucleotide variant	NM_033214.3(GK2):c.1273G>A (p.Asp425Asn)	not specified [RCV004917089]	uncertain significance	4	79406928	79406928	Human		name
598251943	CV3977750	single nucleotide variant	NM_033214.3(GK2):c.1633G>A (p.Gly545Arg)	not specified [RCV005346001]	uncertain significance	4	79406568	79406568	Human		name
598251953	CV3977752	single nucleotide variant	NM_033214.3(GK2):c.1088C>G (p.Ala363Gly)	not specified [RCV005346003]	uncertain significance	4	79407113	79407113	Human		name
598220661	CV3977757	single nucleotide variant	NM_033214.3(GK2):c.1452G>T (p.Met484Ile)	not specified [RCV005340486]	uncertain significance	4	79406749	79406749	Human		name
15177911	CV734736	single nucleotide variant	NM_033214.3(GK2):c.1213C>T (p.Arg405Ter)	not provided [RCV000906756]	likely benign	4	79406988	79406988	Human		name
8625851	CV80975	single nucleotide variant	NM_033214.2(GK2):c.1276G>A (p.Gly426Arg)	Malignant melanoma [RCV000061053]	not provided	4	79406925	79406925	Human		name
8631296	CV86457	single nucleotide variant	NM_033214.2(GK2):c.1495C>T (p.Arg499Cys)	Malignant melanoma [RCV000066548]	not provided	4	79406706	79406706	Human		name
8631297	CV86458	single nucleotide variant	NM_033214.2(GK2):c.1258C>T (p.Arg420Cys)	Malignant melanoma [RCV000066549]	not provided	4	79406943	79406943	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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